Overview

Variant ID 22667
Entrez Gene ID 3899
Gene AFF3 (GeneCards)
Location hg19 2:100452415-100452415
hg38 2:99835953-99835953
Disease Asymptomatic
Method Single cell Sequencing Cell cloning
Mutation(HGVS format) NC_000002.11:g.100452415 T>C (Genome Assembly: GRCh37)

Other information

Exon or Intron NA
Position in protein NA
Amino acid changes in protein NA > NA
Position in cDNA NA
Changes in cDNA NA > NA
mRNA accession NA
mRNA length NA
Reference length 243199373

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0.00003228
EIGEN score -0.2768
CADD Raw score (version 1.3) -0.233808 (Deleterious)
FATHMM raw prediction score 0.10942 (Tolerated)
Deleterious probability by DeFine 0.5267 (Deleterious)
Entrez Gene ID 3899 (NCBI Gene)
Official Gene Symbol AFF3 (GeneCards)
Number of variants in AFF3 in this database 4 (view all the variants)
Full name AF4/FMR2 family member 3
Band 2q11.2
Other IDs Vega: OTTHUMG00000153011
OMIM: 601464
HGNC: HGNC:6473
Ensembl: ENSG00000144218
Other names LAF4, MLLT2-like
Summary This gene encodes a tissue-restricted nuclear transcriptional activator that is preferentially expressed in lymphoid tissue. Isolation of this protein initially defined a highly conserved LAF4/MLLT2 gene family of nuclear transcription factors that may function in lymphoid development and oncogenesis. In some ALL patients, this gene has been found fused to the gene for MLL. Multiple alternatively spliced transcript variants that encode different proteins have been found for this gene. [provided by RefSeq, Jul 2008]

Individual #1

Individual ID 29217587.01 (view all the variants in this individual)
Pubmed ID 29217587
Whose mosaic mutation Normal  
Phenotype 1  
Disease Asymptomatic
OMIM ID

Publication #1: 29217587

Pubmed ID 29217587
Title Different mutational rates and mechanisms in human cells at pregastrulation and neurogenesis.
Journal Science
Publication date 2018.02
Disease Asymptomatic
Number of cases cases of unknown sex: 3;